A Multinational Study Assessing an Oral EGFR Inhibitor, DZD6008 in Patients Who Have Advanced NSCLC With EGFR Mutations (TIAN-SHAN1)
This study is designed to evaluate safety and anti-tumor activity of DZD6008 in patients with advanced NSCLC with EGFR mutations.
Trial Details
- NCT ID
- NCT06905197
- Phase
- PHASE1
- Sponsor
- Dizal Pharmaceuticals
- Status
- RECRUITING
- Cancer Type
- Non-Small Cell (NSCLC) Lung Cancer
- Interventions
- Locations (sample)
- New York, New York, United States|40.71427,-74.00597
- New York, New York, United States|40.71427,-74.00597
- Fairfax, Virginia, United States|38.84622,-77.30637
- Blacktown, New South Wales, Australia|-33.76667,150.91667
- Camperdown, New South Wales, Australia|-33.88965,151.17642
Key Eligibility Criteria
- Patients must be able to provide documented informed consent.
- Aged ≥ 18 years.
- Histologically or cytologically confirmed diagnosis of NSCLC, locally advanced or metastatic, not suitable for curative therapy.
- Documentation of EGFR mutations from a local CLIA-certified laboratory (or equivalent). For Part A monotherapy cohorts and all cohorts of Part B, E…
For full eligibility, visit ClinicalTrials.gov.